<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(1)</volume><submitter>Deng H</submitter><pubmed_abstract>Rheumatoid arthritis (RA) is a chronic, systemic, autoimmune disease that may lead to joint damage, deformity, and disability, if not treated effectively. Hedyotis diffusa Willd (HDW) and its main components have been widely used to treat a variety of tumors and inflammatory diseases. The present study utilized a network pharmacology approach, microarray data analysis and molecular docking to predict the key active ingredients and mechanisms of HDW against RA. Eleven active ingredients in HDW and 180 potential anti-RA targets were identified. The ingredients-targets-RA network showed that stigmasterol, beta-sitosterol, quercetin, kaempferol, and 2-methoxy-3-methyl-9,10-anthraquinone were key components for RA treatment. KEGG pathway results revealed that the 180 potential targets were infl</pubmed_abstract><journal>Scientific reports</journal><pagination>1425</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9877023</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Network pharmacology and experimental validation to identify the potential mechanism of Hedyotis diffusa Willd against rheumatoid arthritis.</pubmed_title><pmcid>PMC9877023</pmcid><pubmed_authors>Jiang J</pubmed_authors><pubmed_authors>Wu L</pubmed_authors><pubmed_authors>Sun W</pubmed_authors><pubmed_authors>Zhang S</pubmed_authors><pubmed_authors>Deng H</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>Network pharmacology and experimental validation to identify the potential mechanism of Hedyotis diffusa Willd against rheumatoid arthritis.</name><description>Rheumatoid arthritis (RA) is a chronic, systemic, autoimmune disease that may lead to joint damage, deformity, and disability, if not treated effectively. Hedyotis diffusa Willd (HDW) and its main components have been widely used to treat a variety of tumors and inflammatory diseases. The present study utilized a network pharmacology approach, microarray data analysis and molecular docking to predict the key active ingredients and mechanisms of HDW against RA. Eleven active ingredients in HDW and 180 potential anti-RA targets were identified. The ingredients-targets-RA network showed that stigmasterol, beta-sitosterol, quercetin, kaempferol, and 2-methoxy-3-methyl-9,10-anthraquinone were key components for RA treatment. KEGG pathway results revealed that the 180 potential targets were infl</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-26T17:31:01.295Z</modification><creation>2025-04-06T15:30:21.344Z</creation></dates><accession>S-EPMC9877023</accession><cross_references><pubmed>36697436</pubmed><doi>10.1038/s41598-022-25579-3</doi></cross_references></HashMap>